Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 33 Records) |
| Query Trace: Diabetes Mellitus and HNF1A[original query] |
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| Genetic prediction of postpartum diabetes in women with gestational diabetes mellitus. Diabetes research and clinical practice 2012 Sep 97 (3): 394-8. Ekelund M, Shaat N, Almgren P, Anderberg E, Landin-Olsson M, Lyssenko V, Groop L, Berntorp |
| A new susceptibility locus for myocardial infarction, hypertension, type 2 diabetes mellitus, and dyslipidemia on chromosome 12q24. Disease markers 2014 2014 291419. Wakil Salma M, Muiya Nzioka P, Tahir Asma I, Al-Najai Mohammed, Baz Batoul, Andres Editha, Mazhar Nejat, Al Tassan Nada, Alshahid Maie, Meyer Brian F, Dzimiri Ndu |
| Associations between the common HNF1A gene variant p.I27L (rs1169288) and risk of type 2 diabetes mellitus are influenced by weight. Diabetes & metabolism 2015 Feb 41 (1): 91-4. Morita K, Saruwatari J, Tanaka T, Oniki K, Kajiwara A, Otake K, Ogata Y, Nakagawa |
| MicroRNA-224 is Readily Detectable in Urine of Individuals with Diabetes Mellitus and is a Potential Indicator of Beta-Cell Demise. Genes 2015 6 (2): 399-416. Bacon Siobhán, Engelbrecht Britta, Schmid Jasmin, Pfeiffer Shona, Gallagher Ross, McCarthy Ailbhe, Burke Marie, Concannon Caoimhín, Prehn Jochen H M, Byrne Maria |
| Circulating ghrelin level is higher in HNF1A-MODY and GCK-MODY than in polygenic forms of diabetes mellitus. Endocrine 2015 May . Nowak Natalia, Hohendorff Jerzy, Solecka Iwona, Szopa Magdalena, Skupien Jan, Kiec-Wilk Beata, Mlynarski Wojciech, Malecki Maciej |
| Genomic Study of Cardiovascular Continuum Comorbidity. Acta naturae 0 7 (3): 89-99. Makeeva O A, Sleptsov A A, Kulish E V, Barbarash O L, Mazur A M, Prokhorchuk E B, Chekanov N N, Stepanov V A, Puzyrev V |
| Successful maintenance on sulphonylurea therapy and low diabetes complication rates in a HNF1A-MODY cohort. Diabetic medicine : a journal of the British Diabetic Association 2015 Oct . Bacon S, Kyithar M P, Rizvi S R, Donnelly E, McCarthy A, Burke M, Colclough K, Ellard S, Byrne M |
| A suppressor locus for MODY3-diabetes. Scientific reports 0 6 33087. Garcia-Gonzalez Miguel A, Carette Claire, Bagattin Alessia, Chiral Magali, Makinistoglu Munevver Parla, Garbay Serge, Prévost Géraldine, Madaras Cécile, Hérault Yann, Leibovici Michel, Pontoglio Mar |
| The HNF1A mutant Ala180Val: Clinical challenges in determining causality of a rare HNF1A variant in familial diabetes. Diabetes research and clinical practice 2017 9 133 142-149. Sagen J V, Bjørkhaug L, Haukanes B I, Grevle L, Molnes J, Nedrebø B G, Søvik O, Njølstad P R, Johansson S, Molven |
| Spectrum of mutations in monogenic diabetes genes identified from high-throughput DNA sequencing of 6888 individuals. BMC medicine 2017 12 15 (1): 213. Bansal Vikas, Gassenhuber Johann, Phillips Tierney, Oliveira Glenn, Harbaugh Rebecca, Villarasa Nikki, Topol Eric J, Seufferlein Thomas, Boehm Bernhard |
| High Prevalence of Diabetes-Predisposing Variants in MODY Genes Among Danish Women With Gestational Diabetes Mellitus. Journal of the Endocrine Society 2017 Jun 1 (6): 681-690. Gjesing Anette P, Rui Gao, Lauenborg Jeannet, Have Christian Theil, Hollensted Mette, Andersson Ehm, Grarup Niels, Sun Jihua, Quan Shi, Brandslund Ivan, Damm Peter, Pedersen Oluf, Wang Jun, Hansen Torb |
| Heterogeneous nature of diabetes in a family with a gain-of-function mutation in the ATP-binding cassette subfamily C member 8 (ABCC8) gene. Endocrine journal 2018 8 65 (10): 1055-1059. Shima Kosuke Robert, Usuda Rika, Futatani Takeshi, Akahori Hiroshi, Kaneko Shuichi, Yorifuji Tohru, Takamura Toshina |
| Genetic basis of early-onset, maturity-onset diabetes of the young-like diabetes in Japan and features of patients without mutations in the major MODY genes: Dominance of maternal inheritance. Pediatric diabetes 2018 6 19 (7): 1164-1172. Yorifuji Tohru, Higuchi Shinji, Kawakita Rie, Hosokawa Yuki, Aoyama Takane, Murakami Akiko, Kawae Yoshiko, Hatake Kazue, Nagasaka Hironori, Tamagawa Nobuyos |
| Maturity onset diabetes of the young (MODY) in Chinese children: genes and clinical phenotypes. Journal of pediatric endocrinology & metabolism : JPEM 2019 6 32 (7): 759-765. Ming-Qiang Zhu, Yang-Li Dai, Ke Huang, Wei Wu, Jun-Fen Fu, Chao-Chun Zou, Guan-Ping Do |
| Maternal genetic contribution to pre-pregnancy obesity, gestational weight gain, and gestational diabetes mellitus. Diabetology & metabolic syndrome 2019 11 37. Beysel Selvihan, Eyerci Nilnur, Ulubay Mustafa, Caliskan Mustafa, Kizilgul Muhammed, Haf?zo?lu Merve, Cakal Erm |
| HNF1A gene p.I27L is associated with early-onset, maturity-onset diabetes of the young-like diabetes in Turkey. BMC endocrine disorders 2019 May 19 (1): 51. Beysel Selvihan, Eyerci Nilnur, Pinarli Ferda Alparslan, Kizilgul Muhammed, Ozcelik Ozgur, Caliskan Mustafa, Cakal Erm |
| Functional characterization of p.Pro409His variant in HNF1A, a hypomorphic mutation involved in pancreatic ?-cell dysfunction. Acta diabetologica 2019 4 56 (8): 883-888. Nocera Donatella, Menniti Miranda, Belviso Stefania, Bond Heather Mandy, Lanzillotta Delia, Spoleti Cristina Barbara, Guagliardi Maria Rosaria, Malatesta Paola, Trapasso Francesco, Irace Concetta, Perrotti Nicola, Iuliano Rodol |
| HNF1A gene p.I27L is associated with co-existing preeclampsia in gestational diabetes mellitus. Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology 2019 12 36 (6): 530-534. Beysel Selvihan, Pinarli Ferda Alparslan, Eyerci Nilnur, Kizilgul Muhammed, Hepsen Sema, Alhan Ali, Kan Seyfullah, Caliskan Mustafa, Bozkurt Erhan, Cakal Erm |
| Whole-exome sequencing in Russian children with non-type 1 diabetes mellitus reveals a wide spectrum of genetic variants in MODY-related and unrelated genes. Molecular medicine reports 2019 Oct . Glotov Oleg S, Serebryakova Elena A, Turkunova Mariia E, Efimova Olga A, Glotov Andrey S, Barbitoff Yury A, Nasykhova Yulia A, Predeus Alexander V, Polev Dmitrii E, Fedyakov Mikhail A, Polyakova Irina V, Ivashchenko Tatyana E, Shved Natalia Y, Shabanova Elena S, Tiselko Alena V, Romanova Olga V, Sarana Andrey M, Pendina Anna A, Scherbak Sergey G, Musina Ekaterina V, Petrovskaia-Kaminskaia Anastasiia V, Lonishin Liubov R, Ditkovskaya Liliya V, Zhelenina Liudmila ?, Tyrtova Ludmila V, Berseneva Olga S, Skitchenko Rostislav K, Suspitsin Evgenii N, Bashnina Elena B, Baranov Vladislav |
| Molecular Genetic Study in a Cohort of Iranian Families Suspected to Maturity-Onset Diabetes of the Young, Reveals a Recurrent Mutation and a High-Risk Variant in the CEL Gene. Advanced biomedical research 2020 9 25. Sarmadi Akram, Mohammadi Aliasgar, Tabatabaei Fatemeh, Nouri Zahra, Chaleshtori Morteza Hashemzadeh, Tabatabaiefar Mohammad Am |
| Low genetic confirmation rate in South Indian subjects with a clinical diagnosis of maturity-onset diabetes of the young (MODY) who underwent targeted next-generation sequencing for 13 genes. Journal of endocrinological investigation 2021 11 45 (3): 607-615. Sampathkumar G, Valiyaparambil P P, Kumar H, Bhavani N, Nair V, Menon U, Menon A, Abraham N, Chapla A, Thomas |
| Polymorphisms in Genes of Lipid Metabolism Are Associated with Type 2 Diabetes Mellitus and Periodontitis, as Comorbidities, and with the Subjects' Periodontal, Glycemic, and Lipid Profiles. Journal of diabetes research 2021 11 2021 1049307. Nicchio Ingra G, Cirelli Thamiris, Nepomuceno Rafael, Hidalgo Marco A R, Rossa Carlos, Cirelli Joni A, Orrico Silvana R P, Barros Silvana P, Theodoro Letícia H, Scarel-Caminaga Raquel |
| Association of type 2 diabetes mellitus and periodontal disease susceptibility with genome-wide association-identified risk variants in a Southeastern Brazilian population. Clinical oral investigations 2021 Jan . Cirelli Thamiris, Nepomuceno Rafael, Goveia Jéssica Marina, Orrico Silvana R P, Cirelli Joni A, Theodoro Letícia Helena, Barros Silvana P, Scarel-Caminaga Raquel |
| Identification of Variants Responsible for Monogenic Forms of Diabetes in Brazil. Frontiers in endocrinology 2022 5 13 827325. Abreu Gabriella de Medeiros, Tarantino Roberta Magalhães, da Fonseca Ana Carolina Proença, Andrade Juliana Rosa Ferreira de Oliveira, de Souza Ritiele Bastos, Soares Camila de Almeida Pereira Dias, Cambraia Amanda, Cabello Pedro Hernan, Rodacki Melanie, Zajdenverg Lenita, Zembrzuski Verônica Marques, Campos Junior Már |
| Identification of monogenic variants in more than ten per cent of children without type 1 diabetes-related autoantibodies at diagnosis in the Finnish Pediatric Diabetes Register. Diabetologia 2022 11 66 (3): 438-449. Harsunen Minna, Kettunen Jarno L T, Härkönen Taina, Dwivedi Om, Lehtovirta Mikko, Vähäsalo Paula, Veijola Riitta, Ilonen Jorma, Miettinen Päivi J, Knip Mikael, Tuomi Tiinamai |
| Monogenic diabetes variants in Emirati women with gestational diabetes are associated with risk of non-autoimmune diabetes within 5 years after pregnancy. Metabolism open 2022 11 16 100213. Daggag Hinda, Gjesing Anette P, Mohammad Alshafi, Ängquist Lars, Shobi Bindu, Antony Suma, Haj Dalia, Al Tikriti Alia, Buckley Adam, Hansen Torben, Barakat Maha |
| Role of monogenic diabetes genes on beta cell function in Italian patients with newly diagnosed type 2 diabetes. The Verona Newly Diagnosed Type 2 Diabetes Study (VNDS) 13. Diabetes & metabolism 2022 1 48 (4): 101323. Bonetti S, Zusi C, Rinaldi E, Boselli M L, Csermely A, Malerba G, Trabetti E, Bonora E, Bonadonna R C, Trombetta |
| Screening of Mutations in Maturity-onset Diabetes of the Young-related Genes and RFX6 in Children with Autoantibody-negative Type 1 Diabetes Mellitus. Journal of clinical research in pediatric endocrinology 2023 12 . Enver ?im?ek, Oguz Cilingir, Tulay Simsek, Sinem Kocagil, Ebru Erzurumluoglu Gokalp, Meliha Demiral, Cigdem Bin |
| Examining the clinical and genetic spectrum of maturity-onset diabetes of the young (MODY) in Iran. Scientific reports 2024 8 14 (1): 19860. Sara Asgarian, Hossein Lanjanian, Shiva Rahimipour Anaraki, Farzad Hadaegh, Maryam Moazzam-Jazi, Leila Najd-Hassan-Bonab, Sajedeh Masjoudi, Asiyeh Sadat Zahedi, Maryam Zarkesh, Bita Shalbafan, Mahdi Akbarzadeh, Sahand Tehrani Fateh, Davood Khalili, Amirabbas Momenan, Narges Sarbazi, Mehdi Hedayati, Fereidoun Azizi, Maryam S Daneshpo |
| Molecular and clinical profiles of pediatric monogenic diabetes subtypes: comprehensive genetic analysis of 138 patients. The Journal of clinical endocrinology and metabolism 2024 11 . Qiaoli Zhou, Sama Samadli, Haoyu Zhang, Xueqin Zheng, Bixia Zheng, Aihua Zhang, Wei |
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